PP andPoster Session, Thursday, June 17Theme F686 - N1123Analytical Solution of an Electrok<strong>in</strong>etic Flow <strong>in</strong> a Nano-Channel us<strong>in</strong>g Curvil<strong>in</strong>ear Coord<strong>in</strong>ates111UMehdi MostofiUP P*, Davood D. GanjiP Mofid Gorji-BandpyP1PDepartment of Mechanical Eng<strong>in</strong>eer<strong>in</strong>g, Noshiravani University of Technology, Babol, IranAbstract-In this paper, an electrok<strong>in</strong>etic flow of an electrolyte <strong>in</strong> a 15 nm radius nano-channel will be studied. This study will be with existenceof the Electric Double Layer (EDL) and fully analytical. Govern<strong>in</strong>g equations for electrok<strong>in</strong>etic phenomena are Poisson-Boltzmann, Navier-Stokes, species and mass conservation equations. Induced electric potential force the electrolyte ions and decrease the mass flow rate. In thispaper, it is assumed that, zeta potential has small quantity. In this paper, after gett<strong>in</strong>g the equations set from the literature and transform<strong>in</strong>g it<strong>in</strong>to curvil<strong>in</strong>ear coord<strong>in</strong>ates, the set will be simplified and be solved analytically for small zeta potentials <strong>in</strong> a nano-channel.One of the most important subsystems of the micro- andnano- fluidic devices is their passage or “Micro- and Nano-Channel”. Nano-channel term is referred to channels withhydraulic diameter less than 100 nanometers [1]. By decrease<strong>in</strong> size and hydraulic diameter some of the physical parameterssuch as surface tension will be more significant while they arenegligible <strong>in</strong> normal sizes.Concentrat<strong>in</strong>g surface loads <strong>in</strong> liquid – solid <strong>in</strong>terface makesthe EDL to be existed. If the loads are concentrated <strong>in</strong> the endof nano-channels, a potential difference will be generated thatforces the ions <strong>in</strong> the nano-channel. However, <strong>in</strong>duced electricfield is discharged by electric conduction of the electrolyte.Rice and Whitehead [2], Lu and Chan [3] and Ke and Liu[4] studied the flow <strong>in</strong> capillary tube. None of them solved theproblem based on the curvil<strong>in</strong>ear coord<strong>in</strong>ates system. Also, allof them studied the problem with existence of the pressuregradient while <strong>in</strong> the modern applications, the pressuregradient can be elim<strong>in</strong>ated and consequently, solv<strong>in</strong>g theproblem consider<strong>in</strong>g this fact is necessary. In this paper, forsmall zeta potentials without pressure gradient will be studiedbased on the curvil<strong>in</strong>ear coord<strong>in</strong>ates <strong>in</strong> a capillary tube.In electrok<strong>in</strong>etic processes, for the most general form of thestudy, seven nonl<strong>in</strong>ear equations govern an electrok<strong>in</strong>eticprocess [5]. In this paper, by some simplifications that will bementioned later, this set will be made simpler.Next <strong>in</strong> this work, a very long nano- tube will be<strong>in</strong>vestigated. Accord<strong>in</strong>g to the fact that reference length of thetube accord<strong>in</strong>g to x direction (L) is very larger than capillaryradius (R) and reference amount for theta ( ), we can neglectseveral terms of the equations. In addition, it is assumed that,electric potential <strong>in</strong> the x direction is constant. Accord<strong>in</strong>g tothese assumptions, the equations mentioned below will beavailable:1 r X p X m2(1)r r r 1r urr r 1 Xrr r r1 Xrr r rpm eE0RT2 F U0Xp Xm(2) Xp 0r(3) X m0r(4)By apply<strong>in</strong>g boundary conditions(no slip condition at walland free stream velocity <strong>in</strong> center of nano-channel for velocityfield and zeta potential at wall and f<strong>in</strong>ite amount of it at centerof the nano-channel for potential field), we have the follow<strong>in</strong>gfigures. Figures (a) and (b) show the results for velocity andpotential fields respectively.In summary, by consider<strong>in</strong>g curvil<strong>in</strong>ear coord<strong>in</strong>ates andus<strong>in</strong>g Taylor series, some derivation of Developed BesselODE has been derived and solved for Poisson-Boltzmannequation. In addition, velocity profile <strong>in</strong> nano-tube has beenachieved for small amounts of zeta potentials. Results thoseare derived by curvil<strong>in</strong>ear coord<strong>in</strong>ates are <strong>in</strong> good agreementwith those of resulted by rectil<strong>in</strong>ear ones <strong>in</strong> [5].Figure 1. Normalized distribution of potential as a function ofnormalized radius.Figure 2. Normalized velocity profile as a function ofnormalized radius.* Correspond<strong>in</strong>g author: HTmehdi_mostofi@yahoo.comT[1] S. Kandlikar, et. al, Heat Transfer and Fluid Flow <strong>in</strong>M<strong>in</strong>ichannels and Microchannels. Elsevier Limited, Oxford (2006).[2] Rice, C.L. and Whitehead, R. J. Phys. Chem., 69(11), 4017–4023(1965)[3] W.Y. Lo, and K. Chan. J. Chem. Phys., 143, 339–353 (1994)[4] H. Keh, and Y.C. Liu, J. Colloids and Interface Surfaces, 172,222–229 (1995)[5] Zheng, Z.: Electrok<strong>in</strong>etic Flow <strong>in</strong> Micro- and Nano- FluidicComponents. Ohio State University, (2003).6th Nanoscience and Nanotechnology Conference, zmir, 2010 681
Poster Session, Thursday, June 17Theme F686 - N1123Multi wall carbon nanotubes as a sensor and p-am<strong>in</strong>ophenol as a mediator for rapid and sensitivedeterm<strong>in</strong>ation of cysteam<strong>in</strong>e <strong>in</strong> presence of tryptophanHassan Karimi-Maleh * Ali A. Ensafi,1 Department of Chemistry, Isfahan university of technology, Isfahan, IranAbstract— In this work, we describe the determ<strong>in</strong>ation of two important biological compounds, cysteam<strong>in</strong>e (CA) andtryptophan (TP) by electrochemical methods us<strong>in</strong>g multi wall carbon nanotubes as a sensor and p-am<strong>in</strong>ophenol as a mediatorfor the first time. The proposed method was successfully applied to the determ<strong>in</strong>ation of CA <strong>in</strong> both capsule andur<strong>in</strong>e samples.Cysteam<strong>in</strong>e (CA) or 2-mercaptoethylam<strong>in</strong>e is the chemicalcompound with the formula HSCH2CH2NH2 [1]. It is thesimplest stable am<strong>in</strong>othiol and a degradation product of theam<strong>in</strong>o acid cyste<strong>in</strong>e. Under the trade name Cystagon,cysteam<strong>in</strong>e is used <strong>in</strong> the treatment of disorders of cyst<strong>in</strong>eexcretion. Cysteam<strong>in</strong>e cleaves the disulfide bond with cyst<strong>in</strong>eto produce molecules that can escape the metabolic defect <strong>in</strong>cyst<strong>in</strong>osis and cyst<strong>in</strong>uria. It is also used for treatment ofradiation sickness [2]. Cysteam<strong>in</strong>e crosses the plasma andlysosomes, and it reacts with crystallized cyst<strong>in</strong>e with<strong>in</strong> thelysosomes to form cyste<strong>in</strong>e and cyste<strong>in</strong>e–cysteam<strong>in</strong>e mixeddisulfides, which leave through the lys<strong>in</strong>e porter [3]. Thecysteam<strong>in</strong>e and its disulfide, cystam<strong>in</strong>e, have been shown tobe neuroprotective <strong>in</strong> a number of cell culture and animalmodels [4]. Tryptophan (TP) is one of the 20 standard am<strong>in</strong>oacids, as well as an essential am<strong>in</strong>o acid <strong>in</strong> the human diet. Itis encoded <strong>in</strong> the standard genetic code as the codon UGG.Several methods have been proposed for the determ<strong>in</strong>ation ofcysteam<strong>in</strong>e and trptophan <strong>in</strong> biological samples <strong>in</strong>clud<strong>in</strong>gchromatography [5,6], electrophoresis [7], gaschromatography with flame photometric detection [8] ionexchange chromatography [9] and electrochemical methods[10, 11] us<strong>in</strong>g modified electrodes. Therefore, <strong>in</strong>cont<strong>in</strong>uation of our studies concern<strong>in</strong>g the preparation ofchemically modified electrodes [12-15], we have usedvoltammetric and electrochemical impedance spectroscopictechniques at pH 5.0 to demonstrate the electrochemicalbehavior of CA and TP on the multi-wall carbon nanotubespaste electrode modified with p-am<strong>in</strong>ophenol as a mediator forthe first time. The results show that the proposed method ishighly selective and sensitive <strong>in</strong> the determ<strong>in</strong>ation of CA andTP out perform<strong>in</strong>g any method reported <strong>in</strong> the literature onelectrochemistry for simultaneous determ<strong>in</strong>ation of these twosubstances. The detection limit, l<strong>in</strong>ear dynamic range, andsensitivity to CA with carbon nanotubes paste electrodemodified with p-am<strong>in</strong>ophenol (p-APMCNTPE) arecomparable to, and even better than, those recently developedwhich use voltammetric methods.Us<strong>in</strong>g differential pulse voltammetry, CA and TA <strong>in</strong> mixturecan each be measured <strong>in</strong>dependently from the other with apotential difference of 600 mV. Us<strong>in</strong>g the modified electrode,the k<strong>in</strong>etics of CA electrooxidation was considerablyenhanced by lower<strong>in</strong>g the anodic overpotential through acatalytic fashion. The mechanism of CA electrochemicalbehavior at the modified electrode surface was analyzed byCyclic voltammetric (CV), chronoamperometric, andelectrochemical impedance spectroscopy (EIS) methods <strong>in</strong> anaqueous solution at pH=5.0. The electrocatalytic currents<strong>in</strong>crease l<strong>in</strong>early with the CA and TP concentrations over theranges 0.5–300 mol L -1 and 10.0–650 mol L -1 , respectively.The detection limits for CA and TP will be equal to 0.15 and5.5 mol L -1 , respectively. The proposed method wassuccessfully applied to the determ<strong>in</strong>ation of CA <strong>in</strong> bothcapsule and ur<strong>in</strong>e samples.*Correspond<strong>in</strong>g author: h.karimi@ch.iut.ac.ir[1] wikipedia. February 06, 2010.[2] B.P. Lukash<strong>in</strong> and A.N. Grebeniuk, Radiatsionnaia biologiia,radioecologiia / Rossiskaia akademiia nauk, 41, 310, 2001.[3] L. Wood et al. Bra<strong>in</strong> Research. 158, 158, 2007.[4] P. Lochman et al. Electrophoresis, 24, 1200, 2003.[5] M. Stachowicz et al. J. Pharm. Biomed. Anal. 17, 767, 1998.[6] H. Kataoka, et. Al. J. Pharm. Biomed. Anal. 11, 963, 1993.[7] A.J. Jonas and J.A. Schneider, Anal.Biochem. 114, 429 1981.[8] H. Kataoka, et. al. J. Chromatogr. B 657, 9, 1994.[9] M. Hsiung et. al. Biochem, Med. 19, 305, 1978.[10] J.B. Raoof et. al. J. Mater. Sci. 44, 2688, 2009.[11] J.B. Raoof. et. al.Electroanalysis, 20, 1259,2008.[12] A.A. Ensafi and H. Karimi-Maleh, J. Elecroanal. Chem. 640, 75, 2010.[13] A.A. Ensafi, et. al. J. Solid State Electrochem. In press.[14] H. Karimi-Maleh, et. al. J. Solid State Electrochem. 14, 9, 2010.[15] H. Karimi-Maleh et. al. J. Braz. Chem. Soc.20, 880, 2009.Figure 1. SEM image of a) p-APMCNTPE, and b) CNPE.6th Nanoscience and Nanotechnology Conference, zmir, 2010 682
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